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Pediatric Rheumatology Online Journal
|
September 12, 2020
A case of Myhre syndrome mimicking juvenile scleroderma
Barbara Jensen, Rebecca James, Ying Hong, et al.
The Journal of Reproductive Medicine
|
December 15, 2006
Value of whole body 18FDG-PET to identify the active site of gestational trophoblastic neoplasia
Tony Dhillon, Carlo Palmieri, Neil J Sebire, et al.
BMJ Paediatrics Open
|
September 2, 2022
Establishing risk factors and outcomes for congenital hypothyroidism with gland in situ using population-based data linkage methods: study protocol
Milagros Ruiz Nishiki, Melissa Cabecinha, Rachel Knowles, et al.
Lancet (London, England)
|
July 2, 2002
Outcome of twin pregnancies with complete hydatidiform mole and healthy co-twin
Neil J Sebire, Marianne Foskett, Fernando J Paradinas, et al.
Plos One
|
August 10, 2018
"We might get a lot more families who will agree": Muslim and Jewish perspectives on less invasive perinatal and paediatric autopsy
Celine Lewis, Zahira Latif, Melissa Hill, et al.
British Medical Bulletin
|
November 28, 2012
Placenta as a reservoir of stem cells: an underutilized resource?
Caterina Pipino, Panicos Shangaris, Elisa Resca, et al.
Molecular Human Reproduction
|
June 1, 2006
Impaired expression of endometrial differentiation markers and complement regulatory proteins in patients with recurrent pregnancy loss associated with antiphospholipid syndrome
Julia Francis, Raj Rai, Neil J Sebire, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 18, 2017
Clinical risk stratification of paediatric renal transplant recipients using C1q and C3d fixing of de novo donor-specific antibodies
Jon Jin Kim, Olivia Shaw, Chloe Martin, et al.
Prenatal Diagnosis
|
March 26, 2017
Learning effect on perinatal post-mortem magnetic resonance imaging reporting: single reporter diagnostic accuracy of 200 cases
Clare Ashwin, J Ciaran Hutchinson, Xin Kang, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 3, 2019
<i>DUOX2</i>/<i>DUOXA2</i> Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom
Catherine Peters, Adeline K Nicholas, Erik Schoenmakers, et al.
Page
of 37
Search research articles
Search
Showing results (241-250 of 369) with videos related to
Sort By:
Page
of 37
Pediatric Rheumatology Online Journal
|
September 12, 2020
A case of Myhre syndrome mimicking juvenile scleroderma
Barbara Jensen, Rebecca James, Ying Hong, et al.
The Journal of Reproductive Medicine
|
December 15, 2006
Value of whole body 18FDG-PET to identify the active site of gestational trophoblastic neoplasia
Tony Dhillon, Carlo Palmieri, Neil J Sebire, et al.
BMJ Paediatrics Open
|
September 2, 2022
Establishing risk factors and outcomes for congenital hypothyroidism with gland in situ using population-based data linkage methods: study protocol
Milagros Ruiz Nishiki, Melissa Cabecinha, Rachel Knowles, et al.
Lancet (London, England)
|
July 2, 2002
Outcome of twin pregnancies with complete hydatidiform mole and healthy co-twin
Neil J Sebire, Marianne Foskett, Fernando J Paradinas, et al.
Plos One
|
August 10, 2018
"We might get a lot more families who will agree": Muslim and Jewish perspectives on less invasive perinatal and paediatric autopsy
Celine Lewis, Zahira Latif, Melissa Hill, et al.
British Medical Bulletin
|
November 28, 2012
Placenta as a reservoir of stem cells: an underutilized resource?
Caterina Pipino, Panicos Shangaris, Elisa Resca, et al.
Molecular Human Reproduction
|
June 1, 2006
Impaired expression of endometrial differentiation markers and complement regulatory proteins in patients with recurrent pregnancy loss associated with antiphospholipid syndrome
Julia Francis, Raj Rai, Neil J Sebire, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 18, 2017
Clinical risk stratification of paediatric renal transplant recipients using C1q and C3d fixing of de novo donor-specific antibodies
Jon Jin Kim, Olivia Shaw, Chloe Martin, et al.
Prenatal Diagnosis
|
March 26, 2017
Learning effect on perinatal post-mortem magnetic resonance imaging reporting: single reporter diagnostic accuracy of 200 cases
Clare Ashwin, J Ciaran Hutchinson, Xin Kang, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 3, 2019
<i>DUOX2</i>/<i>DUOXA2</i> Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom
Catherine Peters, Adeline K Nicholas, Erik Schoenmakers, et al.
Page
of 37